癌症研究
淋巴瘤
生物
自噬
弥漫性大B细胞淋巴瘤
细胞周期
小RNA
DNA损伤
发病机制
细胞周期检查点
免疫系统
基因
免疫失调
DNA修复
细胞凋亡
免疫学
DNA
遗传学
作者
Ting-Xun Lu,Ken H. Young,Wei Xu,Jian-Yong Li
标识
DOI:10.1016/j.critrevonc.2015.08.006
摘要
The aberrations of TP53 gene and dysregulation of the TP53 pathway are important in the pathogenesis of many human cancers, including malignant lymphomas, especially for diffuse large B cell lymphoma (DLBCL). By regulating many downstream target genes or molecules, TP53 governs major defenses against tumor growth and promotes cellular DNA repair, apoptosis, autophagy, cell cycle arrest, signaling, transcription, immune or inflammatory responses and metabolism. Dysfunction of TP53, including microRNA regulations, copy number alterations of TP53 pathway and TP53 itself, dysregulation of TP53 regulators, and somatic mutations by abnormal TP53 function modes, play an important role in lymphoma generation, progression and invasion. The role of TP53 in DLBCL has been widely explored recently. In this review, we summarized recent advances on different mechanisms of TP53 in DLBCL and new therapeutic approaches to overcome TP53 inactivation.
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